Genetic Diseases, Inborn - Holoprosencephaly PubMed MeSh Term

Overview

subject area of

• Novel FGF8 Mutations Associated with Recessive Holoprosencephaly, Craniofacial Defects, and Hypothalamo-Pituitary Dysfunction  Journal Article

broader concept

• Genetic Diseases, Inborn - Chromosome Disorders  PubMed MeSh Term